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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">271</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2019-18-3-145-153</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Relevance and management of secondary hypogammaglobulinema in clinical practice</article-title><trans-title-group xml:lang="ru"><trans-title>Актуальность и методы коррекции вторичной гипогаммаглобулинемии в клинической практике</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2689-0569</contrib-id><name-alternatives><name xml:lang="en"><surname>Balashov</surname><given-names>D. N.</given-names></name><name xml:lang="ru"><surname>Балашов</surname><given-names>Д. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><bold>Dmitri N. Balashov</bold>, PhD, Head of Hematopoietic Stem Cell Transplantation Department № 2,</p><p><italic>117997, Moscow, Samory Mashela st., 1 </italic><italic/></p></bio><bio xml:lang="ru"><p><bold>Балашов Дмитрий Николаевич</bold>, доктор медицинских наук, заведующий отделением трансплантации гемопоэтических стволовых клеток № 2, врач-гематолог</p><p><italic>117997, Москва, ГСП-7, ул. Саморы Машела, 1 </italic></p></bio><email>bala8@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-09-13" publication-format="electronic"><day>13</day><month>09</month><year>2019</year></pub-date><volume>18</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>145</fpage><lpage>153</lpage><history><date date-type="received" iso-8601-date="2019-09-13"><day>13</day><month>09</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-09-13"><day>13</day><month>09</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2019, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2019, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/271">https://hemoncim.com/jour/article/view/271</self-uri><abstract xml:lang="en"><p>Advance protocols for the treatment most of oncology, hematology and some inherited disorders may lead to development severe secondary hypogammaglobulinaemia. Particularly, it is often caused by therapy with monoclonal antibodies binding B-cells (such as rituximab, belimumab, inotuzumab), therapy with inhibitors of tyrosine-kinase (imatinib, desatinib), as well as applying a variety of immunosuppressive and chemotherapy agents (steroids, azathioprine, cyclophosphamide etc.). It should be note, that chronic lymphoid leukemia and multiple myeloma could be complicated with hypogammaglobulinaemia, not only because of specific therapy, but also as features of the diseases. Hematopoietic stems cells transplantation can also lead to development severe and prolonged hypogammaglobulinaemia. This is associated with intensive immune/myeloablative therapy, as well as with immunologic reconstitution after transplantation. Modern intravenous immunoglobulins (IVIG) have a wide repertoire of pathogen-specific activity with high safety profile and constitute essential part of therapy patients with secondary hypogammaglobulinaemia. The paper presents literature review of IVIG usage in various clinical situations, as well as several clinical examples of personal experience.</p></abstract><trans-abstract xml:lang="ru"><p>Современные протоколы терапии многих онкологический, гематологических и некоторых наследственных заболеваний могут приводить к развитию тяжелой вторичной гипогаммаглобулинемии. В частности, причиной ее нередко становятся терапия моноклональными антителами к В-клеткам (ритуксимаб, белимумаб, инотузумаб) и ингибиторами тирозинкиназ (иматиниб, дезатиниб), а также применение целого ряда иммуносупрессивных и химиотерапевтических агентов (глюкокортикостероидов, азатиаприна, циклофосфамида и др.). При хроническом лимфолейкозе и множественной миеломе причиной гипогаммаглобулинемии может быть не только специфическая терапия, но и некоторые особенности самих заболеваний. Трансплантация гемопоэтических стволовых клеток также приводит к развитию тяжелой и длительной гипогаммаглобулинемии. Это ассоциировано как с проводимой интенсивной иммуно-/миелоаблативной терапией, так и с особенностями иммунологической реконституции после проведенного лечения. Современные препараты внутривенных иммуноглобулинов (ВВИГ) обладают широким репертуаром патоген-специфической активности при достаточно высоком профиле безопасности и являются неотъемлемой частью сопроводительной терапии пациентов с вторичной гипогаммаглобулинемией. В работе представлен обзор литературных данных о применении ВВИГ в различных клинических ситуациях,  а также несколько клинических примеров из собственного опыта.</p></trans-abstract><kwd-group xml:lang="en"><kwd>secondary hypogammaglobulinema</kwd><kwd>intravenous immunoglobulin</kwd><kwd>chronic lymphocytic leukemia</kwd><kwd>multiple myeloma</kwd><kwd>hematopoietic stem cell transplantation</kwd><kwd>replacement therapy</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>вторичная гипогаммаглобулинемия</kwd><kwd>внутривенные иммуноглобулины</kwd><kwd>хронический лимфолейкоз</kwd><kwd>множественная миелома</kwd><kwd>трансплантация гемопоэтических стволовых клеток</kwd><kwd>заместительная терапия</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Статья написана при финансовой поддержке компании CSL Behring AG (Швейцария)</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1.	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